- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist /Sr ... issues to GRACS CMC management, as neededDemonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or ... efficacyWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical… more
- Merck & Co. (Rahway, NJ)
- …SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for planning/managing ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which ... includes Global Medical and Scientific Affairs as well as Outcomes Research, and will support Pneumococcal Vaccines.Under the guidance of a senior leader, this… more
- Merck & Co. (North Wales, PA)
- …incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may ... reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programsIn… more
- Boehringer Ingelheim Pharmaceuticals, Inc (Ridgefield, CT)
- …Drug Metabolism & Pharmacokinetics, Translational Medicine & Clinical Pharmacology, CMC, Regulatory Affairs , Patient Safety and Pharmacovigilance to implement ... authorities and will consolidate safety data from nonclinical studies into regulatory submissions as needed. In addition, integrated safety assessments may also… more
- Exponent Inc. (Washington, DC)
- …responsible for Providing technical expertise to our clients related to food science, regulatory affairs , product approvals (GRAS, FAP, AAFCO, novel foods ... is to engage multidisciplinary teams of science, engineering, and regulatory experts to empower clients with solutions that create...Our Opportunity We are currently seeking a Senior Food Scientist for a Senior Manager or Principal … more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Principal Scientist (Associate Director) is responsible for developing and implementing Regulatory ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Principal Scientist (Director) Regulatory CMC is responsible for Regulatory Chemistry Manufacturing & Controls ... management for the assigned portfolio of small molecule or biologic products. The Principal Scientist may also support project team goals and organizational… more
- Merck (Upper Gwynedd, PA)
- **Job Description** GRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist /Sr ... issues to GRACS CMC management, as needed + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company to… more
- Veterans Affairs, Veterans Health Administration (Miami, FL)
- …Clinical Laboratory Scientist : vacareers.va.gov/wp-content/uploads/sites/5/Total-Rewards-of-a-Medical-Technologist-Career-Flyer.pdf The ... The CLS maintains all certifications required of a clinical laboratory scientist . Applies knowledge of compliance requirements for laboratory functions. In addition… more
- ConvaTec (Lexington, MA)
- …work and stakeholder management are critical to success within this role. The principal scientist will apply subject matter expertise in cell culture, tissue ... pivot as new information becomes available. In addition, the principal scientist will be key contributor to...& Technical Labs** to execute testing, as required. + ** Regulatory Affairs ** to collaborate on requirements as… more
- Abbott (Santa Clara, CA)
- …stake holders including clinical project management, clinical operations, biostatistics, data management, regulatory affairs , medical affairs as well as ... Santa Clara, CA, currently has an opportunity for a Principal Clinical Scientist ** to join our ONSITE...analyze statistical analysis plans + Generate documents to support regulatory submissions for Abbott products and/or respond to questions… more
- Merck (North Wales, PA)
- **Job Description** **Role Summary** + The Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I ... organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research, and will support Pneumococcal Vaccines. + Under the guidance of a… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
- AbbVie (North Chicago, IL)
- …with many groups external to PDS&T, for example: Manufacturing Operations, Regulatory Affairs , Quality Assurance, etc. Responsibilities: . Effectively functions ... countries. AbbVie Product Development Science & Technology (PDS&T) is seeking a Principal Research Scientist , Peptide Chemistry to conduct late-stage development… more
- Merck (Rahway, NJ)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for planning/managing real ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more
- Caris Life Sciences (Tempe, AZ)
- …reporting, authoring and approving SOPs, monitoring key quality indicators, and partnering with Regulatory Affairs to ensure compliance. + Support the vision and ... bigger than yourself, Caris is where your impact begins.** **Position Summary** The Principal Curation Scientist , Biomarker & Drug Intelligence, will serve as a… more
- J&J Family of Companies (San Diego, CA)
- …championing patients every step of the way. We are searching for a **Senior Principal Scientist , Computational Multiomics, Precision Measures** , to be in either ... approaches in this setting + Engage with Clinical Development, Global Regulatory Affairs , Data Science & Digital Health, Patient Reported Outcomes, Statistics to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Drug Metabolism & Pharmacokinetics, Translational Medicine & Clinical Pharmacology, CMC, Regulatory Affairs , Patient Safety and Pharmacovigilance to implement ... authorities and will consolidate safety data from nonclinical studies into regulatory submissions as needed. In addition, integrated safety assessments may also… more
